Taneja Nilay, Bersi Matthew R, Baillargeon Sophie M, Fenix Aidan M, Cooper James A, Ohi Ryoma, Gama Vivian, Merryman W David, Burnette Dylan T
Department of Cell and Developmental Biology, Vanderbilt University, Nashville, TN 37232, USA.
Department of Biomedical Engineering, Vanderbilt University, Nashville, TN 37232, USA.
Cell Rep. 2020 Apr 7;31(1):107477. doi: 10.1016/j.celrep.2020.03.041.
The mechanical properties of the actin cortex regulate shape changes during cell division, cell migration, and tissue morphogenesis. We show that modulation of myosin II (MII) filament composition allows tuning of surface tension at the cortex to maintain cell shape during cytokinesis. Our results reveal that MIIA generates cortex tension, while MIIB acts as a stabilizing motor and its inclusion in MII hetero-filaments reduces cortex tension. Tension generation by MIIA drives faster cleavage furrow ingression and bleb formation. We also show distinct roles for the motor and tail domains of MIIB in maintaining cytokinetic fidelity. Maintenance of cortical stability by the motor domain of MIIB safeguards against shape instability-induced chromosome missegregation, while its tail domain mediates cortical localization at the terminal stages of cytokinesis to mediate cell abscission. Because most non-muscle contractile systems are cortical, this tuning mechanism will likely be applicable to numerous processes driven by myosin-II contractility.
肌动蛋白皮层的力学性质在细胞分裂、细胞迁移和组织形态发生过程中调节形状变化。我们发现,调节肌球蛋白II(MII)丝的组成可调整皮层的表面张力,从而在胞质分裂期间维持细胞形状。我们的结果表明,MIIA产生皮层张力,而MIIB作为一种稳定的马达蛋白,其包含在MII异源丝中会降低皮层张力。MIIA产生的张力驱动更快的分裂沟内陷和气泡形成。我们还展示了MIIB的马达结构域和尾部结构域在维持胞质分裂保真度方面的不同作用。MIIB的马达结构域维持皮层稳定性,防止形状不稳定引起的染色体错分离,而其尾部结构域在胞质分裂末期介导皮层定位以介导细胞脱离。由于大多数非肌肉收缩系统都是皮层性的,这种调节机制可能适用于许多由肌球蛋白II收缩性驱动的过程。